Canonical Allele Identifier: CA2685603579
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150950148_150950149insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGCCCCCCCCC , CM000669.2:g.150950148_150950149insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGCCCCCCCCC GRCh38
NC_000007.13:g.150647236_150647237insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGCCCCCCCCC , CM000669.1:g.150647236_150647237insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGCCCCCCCCC GRCh37
NC_000007.12:g.150278169_150278170insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGCCCCCCCCC NCBI36
NG_008916.1:g.32778_32779insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC , LRG_288:g.32778_32779insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000461280.2:n.1715_1716insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
ENST00000684241.1:n.3231+19_3231+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
ENST00000262186.10:c.2398+19_2398+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC MANE Select ENSP00000262186.5:n.2398+19_2398+20insGGGGGGGGGCCCCCCCCCCCCCC...
ENST00000330883.9:c.1378+19_1378+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC ENSP00000328531.4:n.1378+19_1378+20insGGGGGGGGGCCCCCCCCCCCCCC...
ENST00000262186.9:c.2398+19_2398+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC ENSP00000262186.5:n.2398+19_2398+20insGGGGGGGGGCCCCCCCCCCCCCC...
ENST00000330883.8:c.1378+19_1378+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC ENSP00000328531.4:n.1378+19_1378+20insGGGGGGGGGCCCCCCCCCCCCCC...
ENST00000430723.4:c.2069_2070insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC ENSP00000387657.4:p.Thr691GlyfsTer39
ENST00000461280.1:n.1704_1705insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
ENST00000473610.5:n.2049_2050insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
ENST00000532957.5:n.2640_2641insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
NM_000238.3:c.2398+19_2398+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC , LRG_288t1:c.2398+19_2398+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC NP_000229.1:n.2398+19_2398+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCC...
NM_001204798.1:c.1397_1398insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC NP_001191727.1:p.Thr467GlyfsTer39
NM_172056.2:c.2417_2418insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC , LRG_288t2:c.2417_2418insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC NP_742053.1:p.Thr807GlyfsTer39
NM_172057.2:c.1378+19_1378+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC , LRG_288t3:c.1378+19_1378+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC NP_742054.1:n.1378+19_1378+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCC...
XM_011516185.1:c.2098+19_2098+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC XP_011514487.1:n.2098+19_2098+20insGGGGGGGGGCCCCCCCCCCCCCCCCC...
XM_011516186.1:c.2398+19_2398+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC XP_011514488.1:n.2398+19_2398+20insGGGGGGGGGCCCCCCCCCCCCCCCCC...
XM_011516185.2:c.2098+19_2098+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC XP_011514487.1:n.2098+19_2098+20insGGGGGGGGGCCCCCCCCCCCCCCCCC...
XM_011516186.3:c.2398+19_2398+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC XP_011514488.1:n.2398+19_2398+20insGGGGGGGGGCCCCCCCCCCCCCCCCC...
XM_017012195.1:c.2248+19_2248+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC XP_016867684.1:n.2248+19_2248+20insGGGGGGGGGCCCCCCCCCCCCCCCCC...
XM_017012196.1:c.2221+19_2221+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC XP_016867685.1:n.2221+19_2221+20insGGGGGGGGGCCCCCCCCCCCCCCCCC...
NM_000238.4:c.2398+19_2398+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC MANE Select NP_000229.1:n.2398+19_2398+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCC...
NM_001204798.2:c.1397_1398insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC NP_001191727.1:p.Thr467GlyfsTer39
NM_172057.3:c.1378+19_1378+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC NP_742054.1:n.1378+19_1378+20insGGGGGGGGGCCCCCCCCCCCCCCCCCCCC...